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Open AccessJournal ArticleDOI

Spatiotemporal control of gene expression with pulse-generating networks

TLDR
A synthetic multicellular bacterial system where receiver cells exhibit transient gene expression in response to a long-lasting signal from neighboring sender cells that can respond to communication from nearby sender cells while completely ignoring communication from senders cells further away.
Abstract
One of the important challenges in the emerging field of synthetic biology is designing artificial networks that achieve coordinated behavior in cell communities. Here we present a synthetic multicellular bacterial system where receiver cells exhibit transient gene expression in response to a long-lasting signal from neighboring sender cells. The engineered sender cells synthesize an inducer, an acyl-homoserine lactone (AHL), which freely diffuses to spatially proximate receiver cells. The receiver cells contain a pulse-generator circuit that incorporates a feed-forward regulatory motif. The circuit responds to a long-lasting increase in the level of AHL by transiently activating, and then repressing, the expression of a GFP. Based on simulation models, we engineered variants of the pulse-generator circuit that exhibit different quantitative responses such as increased duration and intensity of the pulse. As shown by our models and experiments, the maximum amplitude and timing of the pulse depend not only on the final inducer concentration, but also on its rate of increase. The ability to differentiate between various rates of increase in inducer concentrations affords the system a unique spatiotemporal behavior for cells grown on solid media. Specifically, receiver cells can respond to communication from nearby sender cells while completely ignoring communication from senders cells further away, despite the fact that AHL concentrations eventually reach high levels everywhere. Because of the resemblance to naturally occurring feed-forward motifs, the pulse generator can serve as a model to improve our understanding of such systems.

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Journal ArticleDOI

Network motifs: theory and experimental approaches

TL;DR: Network motifs are reviewed, suggesting that they serve as basic building blocks of transcription networks, including signalling and neuronal networks, in diverse organisms from bacteria to humans.
Journal ArticleDOI

Synthetic biology: applications come of age.

TL;DR: The de novo engineering of genetic circuits, biological modules and synthetic pathways is beginning to address these crucial problems and is being used in related practical applications.
Journal ArticleDOI

The second wave of synthetic biology: from modules to systems

TL;DR: To view cells as true 'programmable' entities, it is now essential to develop effective strategies for assembling devices and modules into intricate, customizable larger scale systems.
Journal ArticleDOI

A synthetic multicellular system for programmed pattern formation

TL;DR: A synthetic multicellular system in which genetically engineered ‘receiver’ cells are programmed to form ring-like patterns of differentiation based on chemical gradients of an acyl-homoserine lactone signal that is synthesized by ‘sender” cells is shown.
Journal ArticleDOI

Synthetic biology: new engineering rules for an emerging discipline

TL;DR: The basic features of synthetic biology as a new engineering discipline are outlined, covering examples from the latest literature and reflecting on the features that make it unique among all other existing engineering fields.
References
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Journal ArticleDOI

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Journal ArticleDOI

A synthetic oscillatory network of transcriptional regulators

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Journal ArticleDOI

Construction of a genetic toggle switch in Escherichia coli

TL;DR: The construction of a genetic toggle switch is presented—a synthetic, bistable gene-regulatory network—in Escherichia coli and a simple theory is provided that predicts the conditions necessary for bistability.
Journal ArticleDOI

Transcriptional Regulatory Networks in Saccharomyces cerevisiae

TL;DR: This work determines how most of the transcriptional regulators encoded in the eukaryote Saccharomyces cerevisiae associate with genes across the genome in living cells, and identifies network motifs, the simplest units of network architecture, and demonstrates that an automated process can use motifs to assemble a transcriptional regulatory network structure.
Journal ArticleDOI

Molecular Bases for Circadian Clocks

TL;DR: It used to be that research in chronobiology moved biochemical functions [transcriptional activators], the along at a gentlemanly pace, but by mid 1997 the word in determining what the authors perceive as time was PASWCCLK.
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